Literature DB >> 33972616

Impact of histological response after neoadjuvant therapy on podocalyxin as a prognostic marker in pancreatic cancer.

Annika Eurola1, Ari Ristimäki2,3, Harri Mustonen1, Anna-Maria Nurmi1, Jaana Hagström2,4, Caj Haglund1, Hanna Seppänen5.   

Abstract

Podocalyxin overexpression associates with poor survival in pancreatic cancer (PDAC). We investigated whether podocalyxin expression correlates with treatment response or survival in neoadjuvant-treated PDAC. Through immunohistochemistry, we evaluated podocalyxin expression in 88 neoadjuvant and 143 upfront surgery patients using two antibodies. We developed a six-tier grading scheme for neoadjuvant responses evaluating the remaining tumor cells in surgical specimens. Strong podocalyxin immunopositivity associated with poor survival in the patients responding poorly to the neoadjuvant treatment (HR 4.16, 95% CI 1.56-11.01, p = 0.004), although neoadjuvant patients exhibited generally low podocalyxin expression (p = 0.017). Strong podocalyxin expression associated with perineural invasion (p = 0.003) and lack of radiation (p = 0.036). Two patients exhibited a complete neoadjuvant response, while a strong neoadjuvant response (≤ 5% of residual tumor cells) significantly associated with lower stage, pT-class and grade, less spread to the regional lymph nodes, less perineural invasion, and podocalyxin negativity (p < 0.05, respectively). A strong response predicted better survival (HR 0.28, 95% CI 0.09-0.94, p = 0.039). In conclusion, strong podocalyxin expression associates with poor survival among poorly responding neoadjuvant patients. A good response associates with podocalyxin negativity. A strong response associates with better outcome.

Entities:  

Year:  2021        PMID: 33972616     DOI: 10.1038/s41598-021-89134-2

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  44 in total

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Journal:  N Engl J Med       Date:  2018-12-20       Impact factor: 91.245

2.  Clinical and histopathological appraisal of preoperative irradiation for adenocarcinoma of the pancreatoduodenal region.

Authors:  O Ishikawa; H Ohhigashi; T Teshima; M Chatani; T Inoue; S Tanaka; T Kitamura; A Wada; Y Sasaki; S Imaoka
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3.  Preoperative Chemoradiotherapy Versus Immediate Surgery for Resectable and Borderline Resectable Pancreatic Cancer: Results of the Dutch Randomized Phase III PREOPANC Trial.

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4.  Cancer statistics, 2020.

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Authors:  Rebekah R White; H Bill Xie; Marcia R Gottfried; Brian G Czito; Herbert I Hurwitz; Michael A Morse; Gerald C Blobe; Erik K Paulson; John Baillie; M Stanley Branch; Paul S Jowell; Bryan M Clary; Theodore N Pappas; Douglas S Tyler
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6.  Randomized phase II study of gemcitabine plus radiotherapy versus gemcitabine, 5-fluorouracil, and cisplatin followed by radiotherapy and 5-fluorouracil for patients with locally advanced, potentially resectable pancreatic adenocarcinoma.

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Journal:  J Surg Oncol       Date:  2010-06-01       Impact factor: 3.454

7.  Preoperative chemoradiation and pancreaticoduodenectomy for adenocarcinoma of the pancreas.

Authors:  D B Evans; T A Rich; D R Byrd; K R Cleary; J H Connelly; B Levin; C Charnsangavej; C J Fenoglio; F C Ames
Journal:  Arch Surg       Date:  1992-11

8.  The Results of Pancreatic Resections and Long-Term Survival for Pancreatic Ductal Adenocarcinoma: A Single-Institution Experience.

Authors:  H Seppänen; A Juuti; H Mustonen; C Haapamäki; S Nordling; M Carpelan-Holmström; J Sirén; J Luettges; C Haglund; T Kiviluoto
Journal:  Scand J Surg       Date:  2016-06-23       Impact factor: 2.360

9.  Neoadjuvant therapy offers longer survival than upfront surgery for poorly differentiated and higher stage pancreatic cancer.

Authors:  Anna Nurmi; Harri Mustonen; Helka Parviainen; Katriina Peltola; Caj Haglund; Hanna Seppänen
Journal:  Acta Oncol       Date:  2017-12-15       Impact factor: 4.089

10.  Preoperative Modified FOLFIRINOX Treatment Followed by Capecitabine-Based Chemoradiation for Borderline Resectable Pancreatic Cancer: Alliance for Clinical Trials in Oncology Trial A021101.

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Journal:  JAMA Surg       Date:  2016-08-17       Impact factor: 14.766

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